Method of producing graphene

ABSTRACT

A method of producing graphene sheets comprising the steps of, forming a carbonaceous powder by electrochemical erosion of a graphite electrode in a molten salt comprising hydrogen ions, recovering the resulting carbonaceous powder from the molten salt liquid, and thermally treating the carbonaceous powder by heating the carbonaceous powder in a non-oxidising atmosphere to produce a thermally treated powder comprising graphene sheets. The method allows high production rates of high purity graphene sheets.

The invention relates to methods of producing graphene sheets, forexample graphene nanosheets, by processes that involves theelectrochemical exfoliation of a graphite electrode, preferably followedby heating in a non-oxidising or reducing environment

BACKGROUND

The term “carbon nanostructures” includes structures such as fullerenes,carbon nanotubes (CNTs), carbon nanofibres, carbon nanoparticles, carbonnanoplates, and graphene. Graphene, in particular, possesses manyextraordinary properties such as high ballistic electron mobility, highthermal conductivity, high Young's modulus, high fracture strength, anda high specific surface area. Recently, graphene-based nanomaterialsthat are, in the literature, variously called graphene, carbonnanoflakes, carbon nanoflowers, carbon nanohorns, carbon nanowalls, orgraphene nanosheets (GNSs), have attracted scientific attention due totheir unique dimensions, structure, and electronic properties, whichmake them promising candidates for many applications. Such structuresshall be referred to in this document as graphene sheets or graphenenanosheets. Possible applications for graphene nanosheets include use inelectron field emitters, electrochemical capacitors, electrode materialfor capacitive deionisation, anode materials for lithium-ion batteries,catalyst supports, biosensors, electrodes for fuel cells, photocatalyticapplications, transparent conducting films and nanocontactors. Otherpotential applications may include or involve corrosion prevention,conducting inks, lubricants, more efficient solar cells, novelantibiotics, and filler in new ultra high performance polymer-, ceramic-and metal-based composites. In addition to these, graphene/semiconductornanocomposites are promising new class of catalysts for thephotodegradation of dye pollutants. Graphene also provides newopportunities to advance water desalination technologies, and challengesthe current existing adsorbents employed for the removal of lowconcentrated contaminants from aqueous solutions. Also, graphenenanosheets can be used as templates for fabrication of othernanostructured materials.

Graphene sheets were produced for the first time in small amounts by an“up to bottom” approach of micromechanical cleavage of highly orientedpyrolytic graphite (HOPG). Later, relatively larger amounts ofchemically modified graphene sheets were produced by a number ofapproaches, all of which made use of HOPG as the starting material andinvolved labour-intensive preparations. More recently there has been afocus on the preparation of graphene sheets using similar methods tothose employed in the production of carbon nanotubes. For example,graphene sheets have been synthesized by chemical vapour deposition(CVD) techniques on a substrate as vertically aligned carbon sheetshaving an average thickness of several nanometres. Graphene sheets havealso been synthesized by plasma enhanced CVD (PECVD), hot-wire CVD,dc-plasma enhanced CVD (dc-PECVD), radiofrequency (rf)-PECVD,inductively coupled PECVD, inductively coupled rf-PECVD, glow dischargePECVD, microwave discharge CVD, electron beam excited PECVD, and also bypyrolysis-based methods.

CVD-based synthesis methods for graphene sheets suffer from lowproduction rates, which can be as low as 32 nm min⁻¹. If a surface areaof 1 m² is used for the CVD process, the rate of graphene production istypically less than 1 g per day. Moreover, these methods require complexequipment. As an alternative to CVD processes, the exfoliation ofgraphite into carbon nanomaterials by room temperature ionic liquids hasbeen subject of a number of studies. It has been shown that theelectrolysis of room temperature ionic liquids with graphite electrodesmay lead to some erosion or exfoliation of the graphite electrodematerial into carbon nanostructures including graphene sheets. However,the rate of the synthesis of graphene in room temperature ionic liquidsis low. Moreover, room temperature ionic liquids are mostly toxic,non-biodegradable and too expensive.

At present, no graphene sheet production process exists that is capableof supplying large amounts of graphene sheets or graphene-basedmaterials. Thus, the development of applications and materials usinggraphene is difficult.

SUMMARY OF INVENTION

The invention provides methods of producing graphene sheets and acarbonaceous powder comprising graphene sheets as defined in theappended independent claims to which reference should now be made.Preferred and/or advantageous features of the invention are set out independent sub-claims.

Thus, in a first aspect a method of producing graphene sheets maycomprise the steps of, (a) forming a carbonaceous powder byelectrochemical erosion of a graphite electrode in a molten salt, themolten salt comprising hydrogen ions, (b) recovering the resultingcarbonaceous powder from the molten salt, and (c) thermally treating thecarbonaceous powder by heating the carbonaceous powder in anon-oxidising or reducing atmosphere to produce a thermally treatedpowder comprising graphene sheets.

The terms graphene sheets or graphene refer to a two-dimensionalcrystalline allotrope of carbon. Graphene may be considered to be a oneatomic layer thick sheet of graphite. As used herein, the terms graphenesheets or graphene also include sheets having a thickness of up to tenatomic layers. Depending on the lateral dimensions of the sheet, thegraphene may be referred to as a graphene sheet or a graphene nanosheet.Graphene nanosheets typically have lateral dimensions, i.e. dimensionsin x and y directions, of between 50 nanometres and 500 nanometres.Graphene sheets may have lateral dimensions of greater than 500nanometres.

The molten salt contains hydrogen either as free hydrogen ions, or as adissolved species which may then ionize to form hydrogen ions. Forexample, the molten salt may comprise dissolved water, lithiumhydroxide, and/or hydrogen chloride, and these dissolved species may bea source of hydrogen ions. Hydrogen may be present in lowconcentrations. For example, the molten salt may contain as little asabout 400 ppm of hydrogen ions.

As used herein, the term carbonaceous powder refers to a powdercomprising carbon nanostructures produced by electrochemical erosion ofa graphite electrode. Such carbon nanostructures typically have maximumdimensions of less than 1000 nanometres, for example less than 500nanometres.

A particularly preferred molten salt comprises lithium chloride, as sucha salt is capable of dissolving water. Lithium chloride has a meltingpoint of about 605° C. Other halide salts of lithium may also beparticularly advantageous. A suitable molten salt may comprise othercation species, however, such as sodium or potassium. For example, alithium chloride-potassium chloride mixture of eutectic composition maybe a suitable molten salt. Such a eutectic has a low melting point ofabout 350° C., which may advantageously allow electrochemical erosion ofa graphite electrode at relatively low temperatures. The molten saltcomprises hydrogen ions. For example, hydrogen may be present in themolten salt as water, hydrogen chloride or hydrogen ions. The hydrogencontaining species, such as water or hydrogen chloride, may ionize inthe molten salt to generate hydrogen ions within the salt.

The electrochemical erosion of a graphite electrode involves thepositioning a graphite electrode, along with a second electrode in amolten salt. The second electrode may also be a graphite electrode. Anelectric potential is applied between the electrodes and a currentflows. The current may be direct current or alternating current. Whenthe graphite electrode is cathodic with respect to the other electrode,positive ions from the ionic liquid migrate to the graphite electrodewhere the ions discharge. If the current is direct current the graphiteelectrode will be a cathode and the second electrode will be an anode.In case of an alternating current, the graphite electrodes wouldalternate between being cathodes and anodes.

It is believed that during electrolysis cations from the molten salt,such as lithium ions and hydrogen ions, are discharged and the atoms ormolecules thus formed are intercalated between layers of the graphitematerial forming the graphite electrode. Intercalated atoms or moleculesmay combine to form compounds, for example, lithium hydride. It isbelieved that this intercalation of species derived from the molten saltcauses the erosion or exfoliation of carbonaceous particles from thegraphite electrode. These particles may be in the form of sheets, discs,flakes or tubes of graphite. The exfoliated material may be a singlegraphite layer thick or, more frequently, may be in the form of a stackthat is multiple graphite layers thick.

It may be preferred that the temperature of the molten salt duringelectrochemical erosion of the electrode is relatively high, in order toincrease production rates of the carbonaceous powder. For example, itmay be advantageous that the temperature is greater than 800° C., forexample about 1000° C.+/−100 ° C., during electrochemical erosion of thegraphite electrode. It may be particularly preferred that the step ofelectrochemical erosion of the graphite electrode takes place in alithium chloride based molten salt containing hydrogen ions, and at atemperature of greater than 800° C. Carbonaceous powder produced byelectrochemical erosion of a graphite electrode at such hightemperatures may advantageously contain a higher proportion of sheets,plates, flakes, and carbon nanoscrolls in which the walls of nanoscrollsare partially unscrolled into graphene nanosheets, and a lowerproportion of carbon tubes, than a powder produced by electrochemicalerosion at lower temperatures.

It may be preferred that the current density at the graphite electrodeis 0.5 Amps per square centimetre (A/cm²) or greater during theelectrochemical erosion of the graphite electrode. The rate ofproduction may be advantageously increased by performing theelectrochemical erosion using a current density of 2 A/cm² plus or minus0.5 A/cm². If stainless steel rods of 0.6 cm in diameter and 70 cm inlength are used to connect the electrodes to the potential leads, anaverage voltage of 6.7 V is required to maintain a constant current of35 A between the electrodes, corresponding to a cathode current densityof about 1.1 A/cm². In this condition, the average potential differencebetween the graphite cathode and a Mo reference electrode immersed inthe molten salt is about −3.0 V.

The graphite electrode may be formed of any suitable graphite material.Graphite materials having larger grain sizes (for example grain sizes ofgreater than 10 microns) and larger crystallite sizes (for examplecrystallite sizes of greater than 30 nanometres) may advantageously forma carbonaceous powder having particles with larger planar sizes. Suchcarbonaceous powder may form graphene sheets of large lateral dimensions(e.g. greater than 500 nm lateral dimensions) after thermal treatment ina non-oxidising atmosphere.

Although specialist grades of graphite may be used, a preferredelectrode may be formed from an industrial grade graphite. Industrialgrade graphite electrodes are readily available at large scales withreasonably low costs. Such electrodes are primarily used as theelectrodes of electric arc and ladle furnaces in the steel industry, andtherefore are readily available in different sizes up to about 3 m longand 0.7 m in diameter. Industrial grade graphite electrodes are made bymixing petroleum coke with coal tar binder, followed by extrusion andbaking to carbonize the binder. The electrodes are finally graphitizedby heating at high temperatures, at which point the carbon atoms arrangeinto graphite. Owing to the raw materials used, and economical issues,industrial grade graphite electrodes can be considered as an ideal rawmaterial for cheap and green graphene production technologies in thefuture. The molten salt, may be brought into contact with a moist gasduring the electrochemical erosion of the graphite electrode. Water fromthe moist gas may then react with the molten salt, to introduce hydrogenions into the molten salt. For example, the electrochemical erosion ofthe graphite electrode may be performed in an electrolysis cell under anatmosphere of moist gas, for example a moist inert gas such as moistargon or moist nitrogen. The molten salt may be sparged with a moist gassuch as moist argon or moist nitrogen.

Contact between the moist gas and the molten salt may be continuous forthe duration of the electrochemical erosion process. Contact between themoist gas and the molten salt may be intermittent during theelectrochemical erosion process, for example a flow of moist gas intothe atmosphere above the molten salt may be switched and off atintervals. Contact between the moist gas and the molten salt may occurfor a predetermined period prior to the electrochemical erosion of thegraphite electrode in order to transfer hydrogen species to the moltensalt.

A preferred method of producing a moist gas is to flow a gas streamover, or through, a water source prior to bringing the moist gas intocontact with the molten salt. The skilled person will be aware ofsuitable methods of generating moist gases.

In preferred embodiments a method of producing graphene sheets comprisesthe steps of, (a) forming a carbonaceous powder by electrochemicalerosion of a graphite electrode in a molten salt, the molten salt beingin contact with a moist gas before and/or during electrochemical erosionof the electrode, (b) recovering the resulting carbonaceous powder fromthe molten salt, and (c) thermally treating the recovered carbonaceouspowder by heating in a non-oxidising or reducing atmosphere to produce athermally treated powder comprising graphene sheets. The moist gas ispreferably a moist inert gas such as moist argon or moist nitrogen. Themoist gas reacts with the molten salt to introduce hydrogen ions intothe molten salt. The moist gas is preferably brought into contact withthe molten salt by flowing a stream of the moist gas over the surface ofthe molten salt before or during electrochemical erosion of the graphiteelectrode, or by sparging the molten salt with the moist gas before orduring electrochemical erosion of the graphite electrode. Water from themoist gas may become dissolved in the molten salt and then ionise tocreate hydrogen ions. Water from the moist gas may react with acomponent of the molten salt to form a hydrogen containing species, forexample HCl, which then ionises to form hydrogen ions.

The molten salt may be in contact with a dry gas during theelectrochemical erosion of the graphite electrode. That is, theatmosphere above the molten salt may not be a moist gas but may be a drygas comprising a mixture of an inert gas, such as argon or nitrogen, andhydrogen. Preferably, hydrogen may be present at a concentration ofbetween 1 and 10 mole percent, for example about 3 or 4 or 5 molepercent. The hydrogen may react with the salt to introduce hydrogen ionsinto the molten salt.

In preferred methods, the graphite electrode is operated such that itbecomes cathodic in polarity during electrochemical erosion. Thegraphite electrode may, for example, become cathodic in polarity inconnection with a counter electrode or anode. The counter electrode isalso arranged in contact with the molten salt and may also be a graphiteelectrode. Anodic oxidation of graphite (such as may occur were thegraphite electrode to be made anodic during exfoliation) may lead to theformation of a significant amount of oxygen-containing groups due to theoveroxidation of the graphite. Exfoliation of graphite electrodes undercathodic conditions may provide the advantage of an absence of oxidizingconditions thereby preventing the generation of oxidation defects in thegraphene product.

More than one graphite electrode may be arranged in contact with themolten salt and each of the more than one graphite electrode may beexfoliated. The use of two or more electrodes may advantageously allowthe production of graphene on a large scale by using a number ofrelatively small sized electrodes. This may be beneficial as a number ofsmaller electrodes may not require high electric currents to producegraphene, with resultant technical and safety advantages. It may bebeneficial, for example, to operate the exfoliation process using anelectrode current density of, say, 2 A/cm². To effect a higherexfoliation rate it may be possible to use a larger graphite electrode.However, to maintain current density within desired levels it would benecessary to increase the overall current that is applied. Theexfoliation of multiple smaller electrodes may allow higher productionrates without the need to use higher electric currents.

As an example, the method may comprise the step of (a) forming acarbonaceous powder by electrochemical erosion of two or more graphiteelectrodes in a molten salt comprising hydrogen ions, each of the two ormore graphite electrodes serves as a cathode in connection with acounter electrode for periods of time in order to effect theelectrochemical erosion. Preferably, the method is operated such thateach graphite electrode is alternately applied as the cathode inconnection with a counter electrode. For example, if the method involvestwo graphite electrodes, a first graphite electrode and a secondgraphite electrode, the first electrode may be employed as a cathode inconnection with a counter electrode (an anode) for a period of time. Thesecond electrode may then be employed as a cathode in connection withthe counter electrode for a period of time. The steps may then berepeated such that the first electrode again becomes a cathode inconnection with the counter electrode. The alternation of the first andsecond electrode may continue for as long as required to achieveexfoliation.

Carbonaceous powder may be recovered from a molten salt by a processinvolving the steps of cooling and solidifying the molten saltcontaining the carbonaceous powder formed by erosion of the graphiteelectrode, and washing the solidified salt from the carbonaceous powder,for example washing using copious amounts of water. The method mayfurther comprise the step of vacuum filtration of the washedcarbonaceous material.

The carbonaceous powder recovered from the molten salt may comprisemetal hydride residues. For example, if the carbonaceous powder isformed by electrochemical erosion of a graphite electrode in a lithiumchloride containing molten salt, the molten salt containing lithium andhydrogen ions, the recovered carbonaceous powder may contain lithiumhydride. Metal carbonate residue, for example lithium carbonate residue,may also form by side reactions. Preferably, any metal hydride or metalcarbonate residues may be removed from the carbonaceous powder by thethermal treatment step.

In preferred embodiments the step of thermally treating the carbonaceouspowder comprises heating of the carbonaceous powder to a temperature ofgreater than 1000° C. in a reducing atmosphere. For example, thecarbonaceous powder may be thermally treated by heating to a temperatureof greater than 1100° C. or 1200° C. in a reducing atmosphere. Amicrowave could also be used.

Preferably the carbonaceous powder is thermally treated by heating tothe temperature of about 1250° C., plus or minus 50° C., in a reducingatmosphere.

The reducing atmosphere may be an atmosphere comprising a reducing gas,for example, an atmosphere comprising a mixture of nitrogen andhydrogen.

In alternative embodiments the carbonaceous powder may be thermallytreated by heating in a low pressure environment. For example, thecarbonaceous powder may be thermally treated by heating when undervacuum. Alternatively, the carbonaceous powder may be thermally treatedby heating in an atmosphere of lower than atmospheric pressurecomprising a reducing gas, for example a mixture of nitrogen andhydrogen.

Preferably the graphene sheets are graphene nanosheets having lateraldimensions of greater than 200 nanometres. For example, the graphenesheets may be graphene nanosheets having lateral dimensions of between200 nanometres and 1000 nanometres.

In a second aspect, the invention may provide a carbonaceous powdercomprising greater than 70% by weight of graphene sheets in which thegraphene sheets have lateral dimensions greater than 200 nanometres.Preferably the carbonaceous powder comprises greater than 80% by weightof graphene sheets, for example greater than 85% by weight of graphenesheets or greater than 90% by weight of graphene sheets or greater than95% by weight of graphene sheets.

Advantageously the rate of production of graphene sheets using a methoddefined herein may be orders of magnitude greater than current methodsof producing graphene. For example, when operating the method usingappropriate erosion temperatures and current densities, and a graphiteelectrode having a surface area of 1 m² in contact with the ionicliquid, graphene sheets may be produced at a rate of greater than 1.5 kgper hour. Thus, graphene sheets may be produced using the inventiondescribed herein at rates greater than 20 kg of graphene sheets, persquare metre of graphite electrode in contact with the ionic liquid, perday (>20 kg/m² Day). Advantageously graphene sheets may be produced atrates greater than 25 kg/m² Day, or greater than 30 kg/m² Day, orgreater than 40 kg/m² Day.

Advantageously, the process may be operated such that graphene sheetsare produced at a rate of greater than 100 kg/m² Day, or greater than200 kg/m² Day.

In a further aspect, a method of producing graphene sheets may comprisethe steps of, (a) forming a carbonaceous powder by electrochemicalerosion of a graphite electrode in an ionic liquid, the ionic liquidcomprising hydrogen ions, (b) recovering the resulting carbonaceouspowder from the ionic liquid, and (c) thermally treating thecarbonaceous powder by heating the carbonaceous powder in anon-oxidising or reducing atmosphere to produce a thermally treatedpowder comprising graphene sheets. The ionic liquid may be a molten saltor may be an organic or aqueous ionic liquid. Preferred or advantageousfeatures of the method may be as set out above in relation to the firstaspect.

In a further aspect, a method of producing graphene sheets may comprisethe steps of, (a) forming a carbonaceous powder by electrochemicalintercalation of a metallic species and a hydrogen species into agraphite electrode arranged in contact with an electrolyte, theelectrolyte comprising the metallic ion species and the hydrogen ionspecies, (b) recovering the resulting carbonaceous powder from theelectrolyte, and (c) thermally treating the carbonaceous powder byheating the carbonaceous powder in a non-oxidising or reducingatmosphere to produce a thermally treated powder comprising graphenesheets. The electrolyte may be a molten salt or may be an organic oraqueous ionic liquid. The metallic ion species is preferably lithium,but may be other metallic such as sodium or potassium ions. Theelectrolyte is preferably a lithium chloride based molten saltcomprising hydrogen ions. Preferred or advantageous features of themethod may be as set out above in relation to the first aspect.

In a further aspect, a method of producing graphene sheets may comprisethe steps of, (a) forming a carbonaceous powder by electrochemicalintercalation of hydrogen into a graphite electrode arranged in contactwith an electrolyte, the electrolyte comprising hydrogen ions, (b)recovering the resulting carbonaceous powder from the electrolyte, and(c) thermally treating the carbonaceous powder by heating thecarbonaceous powder in a non-oxidising or reducing atmosphere to producea thermally treated powder comprising graphene sheets. The electrolytemay be a molten salt or may be an organic or aqueous ionic liquid. Theelectrolyte is preferably a molten salt, for example a lithium chloridebased molten salt, comprising hydrogen ions. Preferred or advantageousfeatures of the method may be as set out above in relation to the firstaspect. In some circumstances the graphene sheets produced byelectrochemical erosion of a graphite electrode may be of high enoughpurity that the step of thermal treatment may be omitted. Thus, in afurther aspect, a method of producing graphene sheets may comprise thesteps of, (a) forming a carbonaceous powder by electrochemical erosionof a graphite electrode in a molten salt, the molten salt comprisinghydrogen ions, and (b) recovering the resulting carbonaceous powdercomprising graphene sheets from the molten salt. It may be particularlypreferred that the graphite electrode is used as a negative electrode(cathode) during the electrochemical erosion. It may be particularlypreferred that the electrochemical erosion occurs under an atmosphereconsisting of a mixture of inert gas- and hydrogen, particularlypreferably a dry inert gas- and hydrogen mixture. It may be preferredthat the molten salt is lithium chloride or lithium chloride based.Preferred or advantageous features of the method may be as set out abovein relation to the first aspect.

In a further aspect, a method of producing graphene sheets may comprisethe steps of, (a) forming a carbonaceous powder by electrochemicalerosion of a graphite electrode in a molten salt, in whichelectrochemical erosion of the graphite electrode is performed under anatmosphere comprising an inert gas and hydrogen, and (b) recovering theresulting carbonaceous powder, which comprises graphene sheets, from themolten salt. Preferably the atmosphere does not contain water. The useof an atmosphere comprising hydrogen in contact with the molten salt mayimprove the production of graphene sheets such that a thermal treatmentstep is not required to produce a high yield of graphene. Grapheneproduced using a moist atmosphere according to embodiments disclosedabove may contain impurities, such as lithium carbonate. The use of adry gaseous atmosphere comprising hydrogen may allow formation of highpurity graphene. The method may comprise the further step of (c)thermally treating the carbonaceous powder by heating the carbonaceouspowder in a non-oxidising atmosphere to produce a thermally treatedpowder comprising graphene sheets. Preferably the atmosphere comprisesan inert gas selected from the list consisting of argon and nitrogen,and hydrogen. Preferably the atmosphere comprises between 2 and 10 molepercent hydrogen, for example about 4 mole percent hydrogen. Preferredor advantageous features of the method may be as set out above inrelation to the first aspect.

In a further aspect, a method of producing graphene sheets may comprisethe steps of, (a) forming a carbonaceous powder by electrochemicalerosion of two or more graphite electrodes in a molten salt comprisinghydrogen ions, in which electrochemical erosion of the graphiteelectrodes is performed under an atmosphere comprising an inert gas andhydrogen, and (b) recovering the resulting carbonaceous powder, whichcomprises graphene sheets, from the molten salt. Preferably, the methodis operated such that each graphite electrode is alternately used as anegative electrode in connection with a positive counter electrode. Forexample, if the method involves two graphite electrodes, a firstgraphite electrode and a second graphite electrode, the first electrodemay be used as a negative electrode (a cathode) in connection with apositive counter electrode (an anode) for a period of time. The secondelectrode may then be used as a cathode in connection with the counterelectrode for a period of time. The steps may then be repeated such thatthe first electrode is used as a cathode in connection with the counterelectrode. The alternation of the first and second electrode maycontinue for as long as required to achieve exfoliation. Preferred oradvantageous features of the method may be as set out above in relationto the first aspect.

Embodiments of the invention may be as defined by one or more of thefollowing numbered clauses.

-   1. A method of producing graphene sheets comprising the steps    of, (a) forming a carbonaceous powder by electrochemical erosion of    a graphite electrode in a molten salt comprising hydrogen ions,    and (b) recovering the resulting carbonaceous powder from the molten    salt liquid.-   2. A method of producing graphene sheets comprising the steps    of, (a) forming a carbonaceous powder by electrochemical erosion of    a graphite electrode in a molten salt comprising hydrogen ions, (b)    recovering the resulting carbonaceous powder from the molten salt    liquid, and (c) thermally treating the carbonaceous powder by    heating the carbonaceous powder in a non-oxidising atmosphere to    produce a thermally treated powder comprising graphene sheets.-   3. A method of producing graphene sheets comprising the steps    of, (a) forming a carbonaceous powder by electrochemical erosion of    a graphite electrode in an ionic liquid, the ionic liquid comprising    hydrogen ions, (b) recovering the resulting carbonaceous powder from    the ionic liquid, and (c) thermally treating the carbonaceous powder    by heating the carbonaceous powder in a non-oxidising or reducing    atmosphere to produce a thermally treated powder comprising graphene    sheets.-   4. A method of producing graphene sheets comprising the steps    of, (a) forming a carbonaceous powder by electrochemical    intercalation of a metallic species and a hydrogen species into a    graphite electrode, the graphite electrode being arranged in contact    with an electrolyte, the electrolyte comprising the metallic species    and the hydrogen species, (b) recovering the resulting carbonaceous    powder from the electrolyte, and (c) thermally treating the    carbonaceous powder by heating the carbonaceous powder in a    non-oxidising or reducing atmosphere to produce a thermally treated    powder comprising graphene sheets.-   5. A method of producing graphene sheets comprising the steps    of, (a) forming a carbonaceous powder by electrochemical    intercalation of hydrogen into a graphite electrode arranged in    contact with an electrolyte, the electrolyte comprising hydrogen    ions, (b) recovering the resulting carbonaceous powder from the    electrolyte, and (c) thermally treating the carbonaceous powder by    heating the carbonaceous powder in a non-oxidising or reducing    atmosphere to produce a thermally treated powder comprising graphene    sheets.-   6. A method of producing graphene sheets comprising the steps    of, (a) forming a carbonaceous powder by electrochemical erosion of    two or more graphite electrodes in a molten salt comprising hydrogen    ions, in which electrochemical erosion of the graphite electrode is    performed under an atmosphere comprising an inert gas and hydrogen,    and (b) recovering the resulting carbonaceous powder, which    comprises graphene sheets, from the molten salt.-   7. A method of producing graphene sheets comprising the steps    of, (a) forming a carbonaceous powder by electrochemical erosion of    a graphite electrode in a molten salt, in which electrochemical    erosion of the graphite electrode is performed under an atmosphere    comprising an inert gas and hydrogen, and (b) recovering the    resulting carbonaceous powder, which comprises graphene sheets, from    the molten salt.-   8. A method according to clause 6 or 7 further comprising the step    of (c) thermally treating the carbonaceous powder by heating the    carbonaceous powder in a non-oxidising atmosphere to produce a    thermally treated powder comprising graphene sheets.-   9. A method according to any preceding clause in which the    atmosphere comprises an inert gas selected from the list consisting    of argon and nitrogen, and hydrogen, preferably between 2 and 10    mole percent hydrogen, for example about 4 mole percent hydrogen,    preferably in which the atmosphere is a dry atmosphere.-   10. A method according to any preceding clause in which the molten    salt comprises lithium chloride.-   11. A method according to any preceding clause in which the molten    salt is in contact with a moist gas during the electrochemical    erosion of the graphite electrode, water from the moist gas either    dissolving in the molten salt or reacting with the molten salt to    introduce hydrogen ions into the molten salt.-   12. A method according to any preceding clause in which    electrochemical erosion of the graphite electrode is performed under    an atmosphere of moist gas, for example in which the molten salt is    shrouded under a flow of moist gas.-   13. A method according to any preceding clause in which the molten    salt is sparged with the moist gas during electrochemical erosion of    the graphite electrode.-   14. A method according to clause 11, 12, or 13 in which the moist    gas is a moist inert gas, for example moist argon or moist nitrogen.-   15. A method according to any of clauses 11 to 14 in which the moist    gas is produced by flowing a gas over, or through, a water source.-   16. A method according to any preceding clause in which the    temperature of the molten salt during the electrochemical erosion of    the graphite electrode is greater than 800° C.-   17. A method according to any of clauses 1 to 10 in which the molten    salt is in contact with a dry gas during the electrochemical erosion    of the graphite electrode, the dry gas comprising an inert gas, such    as argon or nitrogen, and hydrogen.-   18. A method according to any preceding clause in which the molten    salt and the carbonaceous powder is recovered from the molten salt    by a process comprising steps of cooling and solidifying the molten    salt, and washing the solidified salt from the carbonaceous powder.-   19. A method according to clause 18 further comprising the step of    vacuum filtration of the washed carbonaceous material.-   20. A method according to any preceding clause in which the    carbonaceous powder comprises a metal hydride compound prior to the    step of thermal treatment, for example lithium hydride, the metal    species in the metal hydride being derived from the molten salt.-   21. A method according to any preceding clause in which the    carbonaceous powder is thermally treated by heating to a temperature    of greater than 1,000° C., for example to 1250° C.+/−50° C., in a    reducing atmosphere, for example, in a reducing gas atmosphere, for    example an atmosphere comprising a mixture of nitrogen and hydrogen.-   22. A method according to any preceding clause in which the    carbonaceous powder is thermally treated by heating in a low    pressure environment, for example under vacuum, or under a partial    vacuum.-   23. A method according to any preceding clause in which the graphene    sheets are graphene nanosheets having lateral dimensions of greater    than 200 nanometres.-   24. A method according to any preceding clause in which the current    at the graphite electrode during electrochemical erosion of the    electrode is greater than 0.5 A/cm², preferably 2 A/cm² +/−0.5    A/cm².-   25. A method according to any preceding clause in which graphene    sheets are produced at a rate of greater than 1 kg per hour,    preferably greater than 1.5 kg per hour, per square metre of    graphite electrode immersed in the ionic liquid.-   26. A method according to any preceding clause in which the graphite    electrode is cathodic in polarity during electrochemical erosion.-   27 A method according to any preceding clause comprising the step    of; (a) forming a carbonaceous powder by electrochemical erosion of    two or more graphite electrodes in a molten salt comprising hydrogen    ions, each of the two or more graphite electrodes alternately    serving as a negative electrode in connection with a positive    counter electrode for periods of time in order to effect the    electrochemical erosion.-   28. A powder comprising greater than 80% by weight of graphene    sheets produced by a method defined in any of clauses 1 to 27.-   29. A carbonaceous powder comprising greater than 80% by weight    graphene sheets, the graphene sheets having lateral dimensions    greater than 200 nanometres.

SPECIFIC EMBODIMENTS OF THE INVENTION

Specific embodiments of the invention according to one or more aspectdisclosed above will now be described with reference to the figures, inwhich;

FIG. 1a is a schematic illustration of an apparatus for electrochemicalerosion of a graphite electrode to produce a carbonaceous powder;

FIG. 1b is a close up of a portion of the apparatus of FIG. 1illustrating how moist gas is produced;

FIGS. 2a and 2b are scanning electron microscopy (SEM) micrographs ofthe carbonaceous powder formed by electrochemical erosion of a graphiteelectrode, showing a structure of predominantly carbon flakes and carbonplates, FIG. 2a is at low magnification and shows clumps of graphenesheets, FIG. 2b is at much higher magnification shows the clumps aremade up of segments of graphene sheets;

FIGS. 3a, 3b and 3c are transmission electron microscopy (TEM)micrographs showing graphene sheets produced as a result of thermallytreating a carbonaceous powder formed by electrochemical erosion of agraphite electrode; FIG. 3c shows an electron diffraction pattern of asingle graphene sheet;

FIG. 4 illustrates x-ray diffraction patterns produced by (a) thegraphite electrode, (b) carbonaceous powder produced as a result ofelectrochemical erosion of the graphite electrode, and (c) graphenesheets produced by thermally treating the carbonaceous powder;

FIG. 5 illustrates Raman spectra in the range 1100-2000 cm⁻¹ produced by(a) the graphite electrode and (b) graphene sheets produced by thermallytreating the carbonaceous powder produced as a result of electrochemicalerosion of the graphite electrode;

FIG. 6 illustrates Raman spectra in the range 2500-2900 cm⁻¹ produced by(a) the graphite electrode and (b) graphene sheets produced by thermallytreating the carbonaceous powder produced as a result of electrochemicalerosion of the graphite electrode,

FIG. 7 is a schematic illustration of an apparatus for electrochemicalerosion of graphite electrodes to produce a carbonaceous powder,

FIG. 8 shows SEM images of the graphene nanosheets produced by thecathodic exfoliation of the graphite electrodes in molten LiCl under anatmosphere of Ar—H₂, and

FIG. 9 typical bright field TEM micrographs of graphene nanosheetsproduced in molten salt process under a flow of Ar—H₂.

A method of forming graphene sheets according to one or more aspectdisclosed above comprises two main steps. In the first of these steps acarbonaceous powder is formed by the electrochemical erosion of agraphite cathode. In the second of these steps the carbonaceous powderis heated in a non-oxidising atmosphere.

A schematic representation of an apparatus used for the electrochemicalerosion process is shown in FIG. 1a . The apparatus 10 comprises avertical tubular Inconel reactor 20, which is positioned inside aresistance furnace 30. The upper end of the reactor 20 is closed with astainless steel lid 21 sealed with an O-ring 22 and compression fittings23. The lid 21 is equipped with feedthroughs for electrode leads and athermocouple 40 as well as with steel pipes for a gas inlet 51 and a gasoutlet 52.

An anode 60 is formed from a graphite crucible having an internaldiameter of 60 mm and height of 150 mm. A cathode 70 is formed from agraphite rod having a diameter of 15 mm, length of 100 mm, and a weightof 32 g. The anode 60 and the cathode 70 are electrically connected to aDC power supply 80 by electrode leads 61, 71. A water cooling system 90prevents an upper portion of the reactor 20 from overheating.

A disc of ceramic insulation 100 within the graphite crucible separatesthe anode 60 from the cathode 70. The graphite crucible contains anelectrolyte 110 of molten lithium chloride (LiCl) in contact with thegraphite cathode 70 and the anode 60.

The gas inlet 51 is coupled, via a steel pipe 50, to a gas canistercontaining dry argon. A U-bend 53, removably couplable to the steel pipe50, contains water 54. When the U-bend is in position, dry argon bubblesthrough the water within the U-bend before entering the reactor 20 atthe gas inlet 51. The U-bend is shown more clearly in FIG. 1b . Onpassing through the U-bend, the dry argon picks up water vapour andbecomes moist argon. Thus, the atmosphere within the reactor 20 abovethe molten lithium chloride 110 is moist argon that enters through thegas inlet 51 and exits through the gas outlet 52.

In a specific example of an electrochemical erosion, 250 g of anhydrousLiCl was used as an electrolyte. The temperature of the electrolyte 110was monitored by the thermocouple 40 placed inside the graphitecrucible. Initially, the temperature of the electrolyte was raised to770° C., at which temperature LiCl is in a molten state, by a ramp of 5°C. min⁻¹, under a dry argon flow of 20 cm³ min⁻¹. After reaching thistemperature, a U-bend 53, containing water 54, was placed in the path ofthe argon gas through the pipe 50 and the flow of the gas was increasedto 100 cm³ min⁻¹. Electrochemical erosion of the cathode was theneffected by applying a constant direct current of 33.0 A between thecathode 70 and the anode 60 for a period of 50 minutes.

After the electrochemical erosion, the reactor 20 and its contents werecooled to room temperature, and the carbonaceous powder resulting fromthe erosion of the cathode was retrieved from the solidified salt bywashing with copious amounts of distilled water and vacuum filtering.The carbonaceous powder obtained was dried at a temperature of 150° C.for 2 h.

To form the graphene sheets, 10 grams of the dried carbonaceous powderwas heat treated in a horizontal tube furnace under an atmospherecontaining 80% N₂-20% H₂. The temperature within the tube furnace wasraised to 1250° C. at a heating rate of 15° C. min⁻¹ and thistemperature was maintained for 30 min, before the furnace was cooleddown to room temperature.

The resulting product was a black fluffy powder which was studied bydifferent techniques and found to comprise at least 90% graphenenanosheets.

A JEOL 6340F field emission scanning electron microscope (SEM) and a 200kV JEOL 2000FX analytical transmission electron microscope (TEM)equipped with electron diffraction were used for electron microscopyevaluations. A Philips 1710 X-ray diffractometer (XRD) with Cu-Karadiation (k=1.54A°) was used to record the diffraction patterns with astep size and dwell time of 0.05 2θ and 15 s, respectively. Thediffraction patterns recorded were analyzed using the X'Pert High ScorePlus program. Raman data were collected using a Renishaw 1000 Ramanscopewith a He—Ne ion laser of wavelength 633 nm.

FIGS. 2a and 2b are SEM micrographs showing the carbonaceous powderproduced by electrochemical erosion of a graphite cathode in a LiClmolten salt as detailed above.

FIG. 2b shows that powder comprises a multitude of carbon flakes orstacks having lateral dimensions of between 100 nm and 300 nm. Thesestructures are several graphene layers in thickness. By contrast, whenthe experiment detailed above was operated under the same conditions butusing a dry argon atmosphere rather than a moist argon atmosphere, thecarbonaceous powder produced comprised a high proportion of carbonnanotubes and nanoparticles. It is believed that the presence ofhydrogen ions in the electrolyte, derived from the moist argon in theatmosphere, may have caused a difference in the morphology of thecarbonaceous powder produced.

FIGS. 3a, 3b and 3c are TEM micrographs of the graphene nanosheetsproduced by thermally treating the carbonaceous powder resulting fromelectrochemical erosion of the graphite cathode under a moist argonatmosphere as described above. It can be seen that the carbon flakes andstacks of the carbonaceous powder (for example as illustrated in FIG. 2b) have disintegrated into individual sheets of graphene having athickness of only a few atomic layers, many only a single atomic layer,and lateral dimensions of about 100 nm to 300 nm. FIG. 3c shows aselected area electron diffraction pattern derived from a graphenesheet.

FIG. 4 shows X-ray diffraction patterns of the material forming thegraphite cathode (line (a)), the carbonaceous powder formed byelectrochemically eroding the graphite cathode (line (b)), and thegraphene sheets produced by thermal treatment of the carbonaceous powder(line (c)).

The prominent and sharp peak in the profile of the graphite cathodematerial at 2θ=26.441° corresponds to the (002) peak of graphite with aninterlayer distance of 0.337 nm.

The X-ray diffraction pattern of the carbonaceous powder contains the(002) peak of graphite at 2θ=26.485° corresponding to an interlayerdistance of 0.336 nm. This pattern also contains additional peaks thatare due to Li₂CO₃ and LiCl phases. It is assumed that the Li₂CO₃ wasformed by side reactions during the electrochemical process. It is alsoquite possible that a quantity of lithium chloride or lithium hydride istrapped in the microstructure of the carbon product during theelectrolysis, which remains trapped after the washing step as it isinaccessible.

The X-ray diffraction pattern of the graphene sheets shows that theLi₂CO₃ diffraction peaks of the carbonaceous powder are absent, whichindicates the removal of Li₂CO₃ during the heat treatment. Carbon has asublimation point of about 3640° C., whereas Li₂CO₃ has anevaporation/decomposition point of about 1300° C. Thus, the Li₂CO₃ ofthe carbonaceous material has been removed by the thermal treatment in areducing atmosphere. Similarly, LiH dissociates to lithium gas andhydrogen at around 1200° C. The (002) peak of the graphene sheets can bedetected at 2θ=26.427 corresponding to an interlayer distance of 0.337nm.

FIG. 5 shows Raman spectra in the wave number range 1000-2000 cm⁻¹ ofthe material forming the graphite cathode (line (a)), and the graphenesheets produced by thermal treatment of the carbonaceous powder formedby electrochemically eroding the graphite cathode (line (b)).

Raman spectroscopy is a powerful technique to study the structuralproperties of carbon based materials. Both spectra shown in FIG. 5 arecharacterized by the presence of the so-called G band at 1576-1579cm⁻¹and D band at 1326-1332 cm⁻¹. The G-band is related to the vibrationof sp² bonded carbon atoms in a two-dimensional hexagonal lattice, whilethe D-band is associated with structural defects and partiallydisordered carbon structures. The integrated intensity ratio IG/ID ofthe G and D bands is an index corresponding to the crystallinity ofgraphitic carbons.

The IG/ID ratios of the graphite cathode material and the graphenesheets are 3.3 and 1.5, respectively. The D peak may be induced to acertain degree by the edge of graphene sheets. The lower value for theIG/ID ratio in respect of the graphene sheets may, therefore, beattributed to the higher density of graphene edges in the graphenesheets material compared to the graphite cathode material. However, theID/IG ratio for the graphene sheets is still high, and suggests that thegraphene sheets are composed of small crystallites with a large degreeof crystallinity.

FIG. 6 shows Raman spectra in the wave number range 2500-2900 cm⁻¹ ofthe material forming the graphite cathode (line (a)), and the graphenesheets produced by thermal treatment of the carbonaceous powder formedby electrochemically eroding the graphite cathode (line (b)). The 2Dband observed in this wave number range is the overtone of the D band.As observed in FIG. 6, the 2D band of the graphite cathode has ashoulder, which disappears in the 2D band of the graphene sheets.Moreover, the 2D band of the graphene sheets is sharp and asymmetrical,suggesting that the graphene sheets consisted of mostly less than a fewlayers of graphene, i.e. mostly less than 5 layers of graphene.

The experiments described above show that a graphite rod can be erodedin molten LiCl under a cathodic potential, and that the erosion productcan be mainly carbon nanotubes or carbon nanoflakes/stacks of graphenesheets, depending on whether the process is carried out in a dry orhumid inert gas flow, respectively.

The molten salt formation of carbon nanotubes in dry inert gas has beenthe subject of a number of previous studies. The formation of carbonnanotubes is proposed to proceed through a three step mechanisminvolving a) the intercalation of alkali metal from a molten salt intointerlayer spaces between graphite planes of a graphite electrode; b) asignificant increase of mechanical stress at the surface of the graphiteelectrode caused by the intercalated species followed by the surfacedisintegration of the graphite layers into the molten salt, and c)rolling up the graphite layers into tubular structures.

The inventors have determined that the presence of water in theatmosphere above a molten salt changes the nature of the carbonnanostructures that are formed by erosion of a graphite electrode. Whilenot wishing to be bound by theory, the mechanism may be as follows.

Molten LiCl may react with humidity of the moist argon atmosphere toform lithium oxides and hydrogen chloride. The formation of HCl also maylead to the formation of H⁺ cations in the molten salt. The water fromhumidity of the moist argon atmosphere may also dissolve into moltenLiCl, without reacting with LiCl. In this case, water can simplydissolve into LiCl and ionise into H⁺ and O⁻². With this in mind, theformation of the graphene nanosheets by the molten salt erosion of agraphite cathode under a flow of humid Ar may be attributed to theintercalation of lithium and hydrogen into the interlayer spacing ofgraphite basal planes leading to the peeling of graphite to producegraphene nanosheets. Moreover, lithium compounds such as Li₂CO₃ may beformed by side reactions between carbonaceous materials, oxygen andlithium species in the molten salt. When heated at an elevatedtemperature, the lithium compounds are removed, thereby a high yield ofgraphene nanosheets is obtained. The heat treatment may also lead to thefurther splitting of stacks of graphene sheets, creating a higherproportion of individual graphene sheets (or stacks of graphene sheetshaving 10 or fewer atomic layers of thickness).

FIG. 7 illustrates an apparatus 1000 used for the production of graphenesheets using a method according to one or more aspects disclosed above.The apparatus comprises a vertical tubular Inconel reactor 1010 arrangedwithin a resistance furnace 1020. An alumina crucible 1030 with aninternal diameter of 10 cm and height of 16 cm is arranged within thereactor 1010.

1 kg of lithium chloride 1040 is arranged within the alumina cruciblealong with three graphite electrodes. The three graphite electrodesconsist of a first cathode 1051, a second cathode 1052 and an anode1060. All three electrodes are formed from a commercially availableindustrial grade graphite. The first cathode 1051 and the second cathode1052 are rods having a diameter of 13 mm (Goodfellow 809-013-12,diameter 13 mm, length 15 cm, purity 99.997%). The anode 1060 is a rodhaving a diameter of 20 mm and length of 30 cm.

The anode 1060 is coupled to a power supply by means of a steel currentconnector 2010. The first and second cathodes are coupled to the powersupply 1090 by way of steel current connectors 2011, 2012 and a DCcurrent diverter 2000. The current diverter 2000 allows current from thepower supply 1090 to be diverted to either the first cathode 1051 or thesecond cathode 1052.

An inlet 170 into the reactor allows for the flow of a shrouding gasinto the reactor to form an atmosphere over the molten salt 1040. In thepreferred example the shrouding gas consists of argon and 4 mole percenthydrogen. An outlet 1080 allows for outflow of the shrouding gas.

Initially, the temperature within the reactor was raised to about 800°C., where the LiCl is in a molten state, by a ramp of 5° C. min⁻¹, undera flow of 200 cm³ min⁻¹ of gas mixture Ar-4% H₂.

The gas mixture is a dry gas. Then the electrochemical process wascarried out. The DC current diverter was adjusted so that the firstcathode 1051 served as the working electrode, whilst the anode 1060served as a counter electrode. In this condition a constant directcurrent of 40 A, corresponding to a cathode current density of about 0.8A cm⁻², was applied between the first cathode and the anode. After aperiod of 20 minutes the current diverter was operated such that thesecond cathode 1052 was connected to the negative pole of the powersupply and served as the working electrode instead of the first cathode1051. After a further 20 minutes the current diverter was operated againand the first cathode once again acted as the working electrode. Thisprocess was repeated at intervals of 20 minutes and for a total time of180 minutes. Thereafter, the cell was cooled to room temperature, andthe carbonaceous product exfoliated from the cathodes was retrieved fromthe solidified salt by washing with copious amounts of distilled waterand vacuum filtering. The black carbonaceous powder obtained was driedat 100° C. The final product was analysed by various means and found toconsist of 40 g of graphene nanosheets in the form of black fluffypowder. FIG. 8 shows SEM images of the graphene nanosheets. Themicrographs indicate the preparation of high yield randomly orientedgraphene nanosheets with an extremely high quality in appearance. FIG. 9exhibits typical bright field TEM micrographs of the graphenenanosheets. A Selected area diffraction pattern recorded on the edge ofa nanosheet is shown in the left top corner of FIG. 9 exhibiting thetypical six-fold symmetry expected for graphene.

From the results obtained the production rate of graphene was calculatedto be 1 kg/h·m²graphite electrode.

1. A method of producing graphene sheets comprising the steps of, (a)forming a carbonaceous powder by electrochemical erosion of a graphiteelectrode in a molten salt comprising hydrogen ions, (b) recovering theresulting carbonaceous powder from the molten salt liquid, and (c)thermally treating the carbonaceous powder by heating the carbonaceouspowder in a non-oxidising atmosphere to produce a thermally treatedpowder comprising graphene sheets.
 2. A method according to claim 1 inwhich the molten salt comprises lithium chloride.
 3. A method accordingto claim 1 in which the molten salt is in contact with a moist gasduring the electrochemical erosion of the graphite electrode, water fromthe moist gas either dissolving in the molten salt or reacting with themolten salt to introduce hydrogen ions into the molten salt.
 4. A methodaccording to claim 1 in which electrochemical erosion of the graphiteelectrode is performed under an atmosphere of moist gas, wherein themolten salt is shrouded under a flow of moist gas.
 5. A method accordingto claim 1 which the molten salt is sparged with the moist gas duringelectrochemical erosion of the graphite electrode.
 6. A method accordingto claim 3 in which the moist gas is a moist inert gas, for examplemoist argon or moist nitrogen.
 7. A method according to any of claim 3in which the moist gas is produced by flowing a gas over, or through, awater source.
 8. A method according to claim 1 in which the temperatureof the molten salt during the electrochemical erosion of the graphiteelectrode is greater than 800° C.
 9. A method according to claim 1 inwhich the molten salt is in contact with a dry gas during theelectrochemical erosion of the graphite electrode, the dry gascomprising an inert gas comprising argon or nitrogen, and hydrogen. 10.A method according to claim 1 in which the molten salt and thecarbonaceous powder is recovered from the molten salt by a processcomprising steps of cooling and solidifying the molten salt, and washingthe solidified salt from the carbonaceous powder.
 11. A method accordingto claim 10 further comprising the step of vacuum filtration of thewashed carbonaceous material.
 12. A method according to claim 1 in whichthe carbonaceous powder comprises a metal hydride compound prior to thestep of thermal treatment, for example lithium hydride, the metalspecies in the metal hydride being derived from the molten salt.
 13. Amethod according to claim 1 in which the carbonaceous powder isthermally treated by heating to a temperature of greater than 1,000° C.,for example to 1250° C. +/−50° C., in a reducing atmosphere, forexample, in a reducing gas atmosphere comprising a mixture of nitrogenand hydrogen.
 14. A method according to claim 1 in which thecarbonaceous powder is thermally treated by heating in a low pressureenvironment.
 15. A method according to claim 1 in which the graphenesheets are graphene nanosheets having lateral dimensions of greater than200 nanometres.
 16. A method according to claim 1 in which the currentat the graphite electrode during electrochemical erosion of theelectrode is greater than 0.5 A/cm².
 17. A method according to claim 1in which graphene sheets are produced at a rate of greater than 1 kg perhour, per square metre of graphite electrode immersed in the ionicliquid.
 18. A method according to claim 1 in which the graphiteelectrode is cathodic in polarity during electrochemical erosion.
 19. Amethod according to claim 1 in which comprising the step of; (a) forminga carbonaceous powder by electrochemical erosion of two or more graphiteelectrodes in a molten salt comprising hydrogen ions, each of the two ormore graphite electrodes alternately serving as a negative electrode inconnection with a positive counter electrode for periods of time inorder to effect the electrochemical erosion.
 20. A powder comprisinggreater than 80% by weight of graphene sheets produced by a methoddefined in claim
 1. 21. A carbonaceous powder comprising greater than80% by weight graphene sheets, the graphene sheets having lateraldimensions greater than 200 nanometres.
 22. A method of producinggraphene sheets comprising the steps of, (a) forming a carbonaceouspowder by electrochemical erosion of a graphite electrode in an ionicliquid, the ionic liquid comprising hydrogen ions, (b) recovering theresulting carbonaceous powder from the ionic liquid, and (c) thermallytreating the carbonaceous powder by heating the carbonaceous powder in anon-oxidising or reducing atmosphere to produce a thermally treatedpowder comprising graphene sheets.
 23. A method of producing graphenesheets comprising the steps of, (a) forming a carbonaceous powder byelectrochemical intercalation of a metallic species and a hydrogenspecies into a graphite electrode, the graphite electrode being arrangedin contact with an electrolyte, the electrolyte comprising the metallicspecies and the hydrogen species, (b) recovering the resultingcarbonaceous powder from the electrolyte, and (c) thermally treating thecarbonaceous powder by heating the carbonaceous powder in anon-oxidising or reducing atmosphere to produce a thermally treatedpowder comprising graphene sheets.
 24. (canceled)
 25. A method ofproducing graphene sheets comprising the steps of, (a) forming acarbonaceous powder by electrochemical erosion of a graphite electrodein a molten salt, in which electrochemical erosion of the graphiteelectrode is performed under an atmosphere comprising an inert gas andhydrogen, and (b) recovering the resulting carbonaceous powder, whichcomprises graphene sheets, from the molten salt.
 26. A method accordingto claim 25 further comprising the step of (c) thermally treating thecarbonaceous powder by heating the carbonaceous powder in anon-oxidising atmosphere to produce a thermally treated powdercomprising graphene sheets.
 27. A method according to claim 25 in whichthe atmosphere comprises an inert gas selected from the group consistingof argon and nitrogen, and hydrogen, having between 2 and 10 molepercent hydrogen in a dry atmosphere.
 28. (canceled)